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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643261Generated: October 27, 2026

Piperidine → 2-Piperidin-1-yl-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide

https://huagongshe.com/reaction/643261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-chloro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamideHCID 68429657—
SolventAcetoneHCID 180—
SolventAcetonitrileHCID 6342—
Product2-Piperidin-1-yl-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamideHCID 1123491195.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 2-chloro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide (40 mg, 0.115 mmol) in acetone (250 μl) was added to a mixture of piperidine (17.1 μl, 0.173 mmol) and DIPEA (40 μl, 0.229 mmol) in MeCN (250 μl). The resulting reaction mixture was heated and stirred in a microwave oven for 10 min. at 100° C. After cooling to room temperature the volatiles were removed in vacuo and the residue purified on a prep. Gilson HPLC. Pure fractions were collected, evaporated in vauco and dried at 50° C. for 16 hours affording 43.8 mg (75%) of the title compounds as a TFA salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700583B2
Source datasetuspto-grants-2010_04
ORD IDord-b521292d31e14319a593a534ebda5712
Source noteuspto-grants-2010_04